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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2243409Generated: November 4, 2026

Hydrochloric Acid → HCID 178426711, compound

https://huagongshe.com/reaction/2243409

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantNitric AcidHCID 944—
Reactant2-Methyl-5-NitroanilineHCID 7444—
ReactantCyanamideHCID 9864—
SolventIsopropanolHCID 3776—
ProductHCID 178426711HCID 17842671181.5%

Reaction Conditions

Temperature80 °C

Reaction Steps

20 g of 2-Methyl-5-nitroaniline (0.131 mol; 1 eq.), 11.05 g of cyanamide (0.263 mol; 2 eq.) and 80 mL of isopropyl alcohol were placed in a reactor flask. The reaction mixture was heated to 80° C., and 18 mL of concentrated hydrochloric acid was slowly added dropwise within 80 minutes. The reaction mixture was stirred for 1 hour while maintaining the temperature at 80° C. Next, 6 mL of concentrated hydrochloric acid was added dropwise and the reaction mixture was kept at 80° C. for 2 hours. The reaction mixture was cooled down to 60° C. and 10 mL of 65% nitric acid (0.142 mol, 1.08 eq.) was added dropwise and the mixture was left with stirring until it was cooled down to room temperature. The solid product was filtered off, washed with 50 mL of isopropyl alcohol and dried in the air to afford 27.45 g (yield 81.1%) of 1-(2-methyl-5-nitrophenyl)guanidine nitrate, m.p. 203-206° C.; 1H NMR (DMSO-d6, 200 MHz): 2.32 (3H, s, CH3), 7.44 (4H, m, 4×NH), 7.64 (1H, d, J=8.2 Hz, 3-H), 8.09 (1H, d, J=2.5 Hz, 6-H), 8.15 (1H, dd, J=8.2 i 2.5 Hz, 4-H), 9.51 (1H, m, NH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07674901B2
Source datasetuspto-grants-2010_03
ORD IDord-489ca6f9502c4e34a108d3c158d4d7c2
Source noteuspto-grants-2010_03